JP2006528166A5 - - Google Patents

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JP2006528166A5
JP2006528166A5 JP2006520908A JP2006520908A JP2006528166A5 JP 2006528166 A5 JP2006528166 A5 JP 2006528166A5 JP 2006520908 A JP2006520908 A JP 2006520908A JP 2006520908 A JP2006520908 A JP 2006520908A JP 2006528166 A5 JP2006528166 A5 JP 2006528166A5
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infection
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生物膜形成を特徴とする細菌感染症を処置する目的で、(i)1若しくはそれ以上のバクテリオファージ、及び(ii)1若しくはそれ以上の抗生物質、を同時、別個、又は連続投与するための複合製品の製造における、(i)及び(ii)の使用。   For the simultaneous, separate or sequential administration of (i) one or more bacteriophages and (ii) one or more antibiotics for the purpose of treating a bacterial infection characterized by biofilm formation Use of (i) and (ii) in the manufacture of composite products. 単一の複合バクテリオファージ調製物の製造において2以上のバクテリオファージを用いる、請求項1記載の使用。   Use according to claim 1, wherein two or more bacteriophages are used in the production of a single complex bacteriophage preparation. 前記複合バクテリオファージ調製物が、同じ細菌種に感染しうる複数種のバクテリオファージを含み、該複数種のバクテリオファージの各メンバーがそれぞれ異なる株特異性を有する、請求項2記載の使用。   The use according to claim 2, wherein the complex bacteriophage preparation comprises a plurality of bacteriophages capable of infecting the same bacterial species, each member of the plurality of bacteriophages having a different strain specificity. 1若しくはそれ以上の抗生物質が、1若しくはそれ以上のバクテリオファージより後に投与される、請求項1〜3のいずれか1項に記載の使用。   4. Use according to any one of claims 1 to 3, wherein the one or more antibiotics are administered after the one or more bacteriophages. 前記細菌感染症が緑膿菌(Pseudomonas aeruginosa)を含むか又はそれからなる、請求項1〜4のいずれか1項に記載の使用。   Use according to any one of claims 1 to 4, wherein the bacterial infection comprises or consists of Pseudomonas aeruginosa. 前記感染症が、皮膚熱傷部若しくは他の皮膚創傷部の感染症、肺感染症、眼感染症又は耳感染症から選択される感染症である、請求項5記載の使用。   6. Use according to claim 5, wherein the infection is an infection selected from infections of skin burns or other skin wounds, lung infections, eye infections or ear infections. 前記感染症がイヌの耳感染症である、請求項6記載の使用。   7. Use according to claim 6, wherein the infection is a dog ear infection. 前記投与が予防的処置のためのものである、請求項1〜5のいずれか1項に記載の使用。   6. Use according to any one of claims 1 to 5, wherein the administration is for prophylactic treatment. 前記複合製品が、コンタクトレンズ用溶液又は添加剤である、請求項8記載の使用。   Use according to claim 8, wherein the composite product is a contact lens solution or additive. NCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179、NCIMB41180及びNCIMB41181(National Collection of Industrial and Marine Bacteria、Aberdeen、英国、に寄託されている)、並びに緑膿菌(P. aeruginosa)を標的とする能力を保持するこれらの変異株から選択される1若しくはそれ以上のバクテリオファージを用いる、請求項5〜9のいずれか1項に記載の使用。   NCIMB41174, NCIMB41175, NCIMB41176, NCIMB41177, NCIMB41178, NCIMB41179, NCIMB41180 and NCIMB41181 (deposited in the National Collection of Industrial and Marine Bacteria, Aberdeen, UK), and P. aeruginosa targeting Use according to any one of claims 5 to 9, wherein one or more bacteriophages selected from these mutant strains to be retained are used. バクテリオファージの集団が用いられ、該集団の各メンバーは、それぞれ異なる株特異性を有し、且つNCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178及びNCIMB41179、NCIMB41180及びNCIMB41181、並びに緑膿菌(P. aeruginosa)を標的とする能力を保持するこれらの変異株から選択される、請求項10記載の使用。   A population of bacteriophages is used, each member of which has a different strain specificity and is NCIMB 41174, NCIMB 41175, NCIMB 41176, NCIMB 41177, NCIMB 41178 and NCIMB 41179, NCIMB 41180 and NCIMB 41181, and P. aeruginosa 11. Use according to claim 10, selected from these mutants which retain the ability to target 用いられるバクテリオファージの集団が、NCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179よりなるか、又は前記のバクテリオファージのいずれかが所望の標的株特異性を示すその変異株に置換されている点で前記集団とは異なる集団である、請求項11記載の使用。   In that the bacteriophage population used consists of NCIMB 41174, NCIMB 41175, NCIMB 41176, NCIMB 41177, NCIMB 41178, NCIMB 41179, or any of the bacteriophages has been replaced by a variant thereof exhibiting the desired target strain specificity. 12. Use according to claim 11, wherein the population is different from the population. 前記バクテリオファージの集団が、イヌの耳感染症の処置での使用ための単一の複合バクテリオファージ調製物の製造において用いられる、請求項12記載の使用。   13. Use according to claim 12, wherein the bacteriophage population is used in the manufacture of a single composite bacteriophage preparation for use in the treatment of canine ear infections. 1若しくはそれ以上のバクテリオファージと、同時、別個又は連続投与するためのアルギナーゼの使用をさらに含む、請求項1〜13のいずれか1項に記載の使用。   14. Use according to any one of claims 1 to 13, further comprising the use of arginase for simultaneous, separate or sequential administration with one or more bacteriophages. National Collection of Industrial and Marine Bacteria、Aberdeen、英国、に寄託されているバクテリオファージ株NCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179、NCIMB41180及びNCIMB41181、又は緑膿菌(P. aeruginosa)を標的とする能力を保持するこれらの変異株から選択されるバクテリオファージ。   Targets the bacteriophage strains NCIMB41174, NCIMB41175, NCIMB41176, NCIMB41177, NCIMB41178, NCIMB41179, NCIMB41180 and NCIMB41181, or P. aeruginosa, deposited in the National Collection of Industrial and Marine Bacteria, Aberdeen, UK A bacteriophage selected from these mutant strains. 請求項15記載の1若しくはそれ以上のバクテリオファージを製薬用担体又は希釈剤と共に含む、医薬組成物。   16. A pharmaceutical composition comprising one or more bacteriophages according to claim 15 together with a pharmaceutical carrier or diluent. 緑膿菌(Pseudomonas aeruginosa)を含むか又はそれからなる細菌感染症を処置する目的で、バクテリオファージの集団を同時、別個、又は連続投与するための複合製品であって、該集団の各メンバーはそれぞれ異なる株特異性を有し、且つ該集団が、NCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179、NCIMB41180、NCIMB41181及び緑膿菌を標的とする能力を保持するこれらの変異株から選択される2若しくはそれ以上のバクテリオファージからなる、上記複合製品。   A combined product for the simultaneous, separate or sequential administration of a bacteriophage population for the purpose of treating a bacterial infection comprising or consisting of Pseudomonas aeruginosa, each member of the population 2 or selected from these strains having different strain specificity and wherein the population retains the ability to target NCIMB41174, NCIMB41175, NCIMB41176, NCIMB41177, NCIMB41178, NCIMB41179, NCIMB41180, NCIMB41181 and Pseudomonas aeruginosa The above complex product consisting of more bacteriophages. 前記バクテリオファージの集団が、バクテリオファージNCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179よりなるか、又は前記のバクテリオファージのいずれかが所望の標的株特異性を示すその変異株に置換されている点で前記集団とは異なる集団である、請求項17記載の複合製品。   The bacteriophage population consists of bacteriophages NCIMB41174, NCIMB41175, NCIMB41176, NCIMB41177, NCIMB41178, NCIMB41179, or any of the bacteriophages has been replaced with a mutant exhibiting the desired target strain specificity 18. The composite product of claim 17, wherein the product is a group different from the group. 前記バクテリオファージの集団を製薬用担体又は希釈剤と共に含む単一の医薬組成物である、請求項17又は18記載の複合製品。   19. A complex product according to claim 17 or 18, which is a single pharmaceutical composition comprising the population of bacteriophages together with a pharmaceutical carrier or diluent. 1若しくはそれ以上のバクテリオファージに対して、同時、別個、又は連続投与するための1若しくはそれ以上の抗生物質を更に含む、請求項16〜19のいずれか1項に記載の組成物又は複合製品。   20. A composition or complex product according to any one of claims 16 to 19, further comprising one or more antibiotics for simultaneous, separate or sequential administration to one or more bacteriophages. . 1若しくはそれ以上のバクテリオファージに対して、同時、別個、又は連続投与するためのアルギナーゼを更に含む、請求項16〜20のいずれか1項に記載の組成物又は複合製品。   21. A composition or composite product according to any one of claims 16 to 20, further comprising arginase for simultaneous, separate or sequential administration to one or more bacteriophages. 緑膿菌(P. aeruginosa)を含むか又はそれからなる細菌感染症を処置するための医薬の製造における、請求項16〜21のいずれか1項に記載の組成物又は複合製品の使用。   Use of a composition or composite product according to any one of claims 16 to 21 in the manufacture of a medicament for treating a bacterial infection comprising or consisting of P. aeruginosa. 前記感染症が、皮膚熱傷部若しくは他の皮膚創傷部の感染症、肺感染症、眼感染症又は耳感染症から選択される感染症である、請求項22記載の使用。   23. Use according to claim 22, wherein the infection is an infection selected from infections of skin burns or other skin wounds, lung infections, eye infections or ear infections. 前記感染症がイヌの耳感染症である、請求項23記載の使用。   24. Use according to claim 23, wherein the infection is a canine ear infection. 前記医薬が予防的処置のために用いられる、請求項22記載の使用。   23. Use according to claim 22, wherein the medicament is used for prophylactic treatment. 生物膜形成を特徴とする細菌汚染を排除、軽減、又は防止する非治療的方法であって、該汚染の細菌を標的とすることが可能な1若しくはそれ以上のバクテリオファージ及びそれと同時、別個、又は連続に1若しくはそれ以上の抗生物質又は消毒剤を、該汚染部位又はその予測部位に適用することを含む、上記方法。   A non-therapeutic method of eliminating, mitigating or preventing bacterial contamination characterized by biofilm formation, wherein one or more bacteriophages capable of targeting the contaminating bacteria and simultaneously, separately; Or continuously applying one or more antibiotics or disinfectants to the site of contamination or its predicted site. 請求項10〜12のいずれか1項に規定される1若しくはそれ以上のバクテリオファージを用いる、請求項26記載の方法。   27. A method according to claim 26, wherein one or more bacteriophages as defined in any one of claims 10-12 are used. 緑膿菌(P. aeruginosa)を含むか又はそれからなる細菌汚染を排除、軽減、又は防止する非治療的方法であって、請求項10〜12のいずれか1項に規定される1若しくはそれ以上のバクテリオファージを該汚染部位又はその予測部位に適用することを含む、上記方法。   13. A non-therapeutic method for eliminating, reducing or preventing bacterial contamination comprising or consisting of P. aeruginosa, comprising one or more as defined in any one of claims 10-12 Applying said bacteriophage to said contaminated site or predicted site thereof. in vitroサンプル中の緑膿菌(P. aeruginosa)の存在を検出する方法であって、該サンプルを請求項10〜12のいずれか1項に規定される1若しくはそれ以上のバクテリオファージと接触させ、そして該バクテリオファージがサンプル中の細菌を死滅させることが可能かどうか決定することを含む、上記方法。   A method for detecting the presence of P. aeruginosa in an in vitro sample, wherein the sample is contacted with one or more bacteriophages as defined in any one of claims 10-12. And determining whether the bacteriophage is capable of killing bacteria in the sample. バクテリオファージNCIMB41174、NCIMB41175、NCIMB41176、NCIMB41177、NCIMB41178、NCIMB41179、NCIMB41180及びNCIMB41181のうち1種類に対して選択的な細菌株を特定する方法であって、いくつかの細菌株での該バクテリオファージによるプラーク形成を測定するステップ、及び前記の他のバクテリオファージよりも該バクテリオファージによって少なくとも1000倍多くのプラーク形成がなされる株を選択するステップを含む、上記方法。   Bacteriophage NCIMB41174, NCIMB41175, NCIMB41176, NCIMB41177, NCIMB41178, NCIMB41179, NCIMB41180 and NCIMB41181, a method for identifying a bacterial strain selective for one of the bacterial strains, and plaque formation by the bacteriophage in several bacterial strains And selecting a strain that produces at least 1000 times more plaque formation by said bacteriophage than said other bacteriophage. 請求項30記載の方法により特定される細菌株。   A bacterial strain identified by the method of claim 30. 治療用途を意図する調製物中に存在するバクテリオファージを特定及び/若しくは定量するため、並びに/又は該治療用途中若しくはその後に取得した組織サンプル中に存在する株を特定するための、請求項31記載の1若しくはそれ以上の細菌株の使用。 32. To identify and / or quantify bacteriophages present in a preparation intended for therapeutic use and / or to identify strains present in tissue samples obtained during or after said therapeutic use. Use of one or more bacterial strains as described.
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